← Back to catalogue

EaglePlug

FDA UDI

Class U (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
EaglePlug FDA UDI
Generic Name
Lacrimal punctum plug FDA UDI
Device Name
EaglePlug Punctum Plug 0.8mm D - 2 per box FDA UDI
Model / Reference
30382 FDA UDI
Description
EaglePlug Punctum Plug 0.8mm D - 2 per box FDA UDI

Identifiers

Catalog Number
30382 FDA UDI
Primary DI / UDI-DI
00841668114582 FDA UDI
510(k) Number
K991130 FDA UDI
FDA Product Code
LZU FDA UDI
GMDN Term
Lacrimal punctum plug FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lacrimal punctum plug

EaglePlug by Katena Products, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lacrimal punctum plug.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 90bd9038-f05d-466e-bbf1-de6abb2dd7f9 36 fields · synced Jun 12, 2026